13016-17-6 Usage
Description
4-methyl-1,3-oxazole-2(3H)-thione, also known as 4-methylisothiazole, is a sulfur-containing heterocyclic compound with the molecular formula C4H5NOS. It is a derivative of the five-membered ring oxazole and is commonly used as a building block in organic synthesis.
Uses
Used in Pharmaceutical and Agrochemical Industries:
4-methyl-1,3-oxazole-2(3H)-thione is used as a precursor for the synthesis of pharmaceuticals and agrochemicals due to its versatile chemical properties and potential for creating a wide range of compounds.
Used as an Antimicrobial Preservative:
4-methyl-1,3-oxazole-2(3H)-thione is used as an antimicrobial preservative in various consumer products such as cosmetics, personal care products, and household cleaners, thanks to its antimicrobial properties.
Used in the Development of New Antimicrobial Agents:
4-methyl-1,3-oxazole-2(3H)-thione is being studied for its potential use in the development of new antimicrobial agents, indicating its importance in the ongoing search for effective treatments against resistant microbes.
While 4-methyl-1,3-oxazole-2(3H)-thione is generally regarded as safe for use in consumer products, further studies on its potential environmental and human health impacts are still ongoing to ensure its safe and responsible use.
Check Digit Verification of cas no
The CAS Registry Mumber 13016-17-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,0,1 and 6 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 13016-17:
(7*1)+(6*3)+(5*0)+(4*1)+(3*6)+(2*1)+(1*7)=56
56 % 10 = 6
So 13016-17-6 is a valid CAS Registry Number.
13016-17-6Relevant articles and documents
Synthesis and antimicrobial evaluation of oxazole-2(3H)-thione and 2-alkylsulfanyl-1,3-oxazole derivatives
Silva, Sandrina,Silva, Filipa V. M.,Justino, Jorge,Rauter, Amelia Pilar,Rollin, Patrick,Tatibouet, Arnaud
, p. 1013 - 1028 (2014/01/17)
The preparation of oxazole-2(3H)-thiones (OXTs) by condensation of thiocyanic acid on α-hydroxycarbonyl substrates has been revisited. Extension to more complex scaffolds afforded chiral OXTs, whereas carbohydrate-fused 2-alkylsulfanyl-1,3-oxazolines led
Nematicidal trifluorobutenes
-
, (2008/06/13)
The present invention relates to novel trifluorobutenes of the formula (I) 1wherein R1 represents hydrogen, halogen, or alkyl which may be unsubstituted or substituted with halogen, hydroxy, alkoxy, alkylthio, alkylcarbonyloxy, haloalkylcarbonyloxy or cyano, or represents alkylsulfonyloxy or represents phenyl which may be unsubstituted or substituted with halogen, alkyl, haloalkyl, alkoxy, alkylthio, alkylsulfonyl, haloalkoxy, haloalkylthio, phenyl, phenoxy, cyano or nitro. R2 represents hydrogen, halogen, or alkyl which may be unsubstituted or substituted with alkoxy or halogen, or represents alkoxycarbonyl, and n represents 0, 1 or 2, provided that if R1 represents alkyl, R2 does not represent halogen, processes for their preparation and their use as nematicides.
On glucosides from imidazol-, oxazol- and thiazolethiones-(2). 30. On the "glycosides from heterocyclic" compounds
Nuhn,Wagner
, p. 186 - 200 (2007/10/09)
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